medical MODERATE Updated 2026-02-18

Elekta, Inc. recalls Brand Name: Leksell GammaPlan Product Name: Radionuclide RT

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Recalled Product

Brand Name: Leksell GammaPlan Product Name: Radionuclide RT Treatment planning system Software Version: 11,3, 11.4 Product Description: Leksell GammaPlan¿ is a computer-based system designed for Leksell Gamma Knife¿ treatment planning.

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Hazard / Issue

Due to an error when defining a new stereotactic reference that users fail to first change an already defined obsolete reference to a pre-plan reference. This may result in a treatment plan that potentially irradiates the incorrect patient location if the error is not detected by users.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: Lot Code: 07340048311878 (LGP 11.3) 07340201502136 (LGP 11.4)

✅ What Should You Do?

  1. 1Contact your healthcare provider immediately to discuss this recall.
  2. 2Stop using the device if it is safe to do so, and contact your provider.
  3. 3Follow the manufacturer's remedy instructions provided in the recall notice.
  4. 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.

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